Thormodsson F R, Antonian E, Grafstein B
Department of Physiology, Cornell University Medical College, New York, New York 10021.
Exp Neurol. 1992 Sep;117(3):260-8. doi: 10.1016/0014-4886(92)90135-d.
A prominent group of soluble glycoproteins with a molecular weight of 30K-40K and pI 5.0-5.6 was detected in various parts of the goldfish brain as well as in the optic nerves. Since these proteins are readily liberated from the tissue, we have designated them exoglycoproteins (X-GPs). The X-GPs in the optic tectum were found to be labeled after intraocular injection of radioactive tracers, in a manner consistent with the labeling of proteins transported in the optic axons. However, the labeling of X-GPs was blocked by intracranial injection of a protein synthesis inhibitor, whereas the labeling of axonally transported proteins was unaffected. This shows that the X-GPs can be synthesized locally within the brain. Nevertheless, when protein synthesis in the retina was blocked, the labeling of the X-GPs in the tectum was prevented, like the labeling of axonally transported proteins. Thus precursors for the synthesis of X-GPs can be derived from materials transported in the optic axons. This synthesis can occur in nonneuronal cells, as indicated by the incorporation of labeled amino acid into X-GPs in optic nerves directly exposed to the label. The synthesis of X-GPs was increased in regenerating nerves, suggesting that these proteins may play a role in regeneration. Partial amino acid sequencing of the proteins showed that they are identical to the proteins previously identified as "ependymins," which have been implicated in neuronal plasticity. There are minor differences in amino acid sequence among some individual spots.
在金鱼脑的各个部位以及视神经中检测到一组显著的可溶性糖蛋白,其分子量为30K - 40K,等电点为5.0 - 5.6。由于这些蛋白质很容易从组织中释放出来,我们将它们命名为外糖蛋白(X - GPs)。发现眼内注射放射性示踪剂后,视顶盖中的X - GPs会被标记,其方式与视神经轴突中运输的蛋白质的标记方式一致。然而,颅内注射蛋白质合成抑制剂会阻断X - GPs的标记,而轴突运输蛋白质的标记不受影响。这表明X - GPs可以在脑内局部合成。尽管如此,当视网膜中的蛋白质合成被阻断时,顶盖中X - GPs的标记也会像轴突运输蛋白质的标记一样被阻止。因此,X - GPs合成的前体可以来源于视神经轴突中运输的物质。这种合成可以在非神经元细胞中发生,直接暴露于标记物的视神经中标记氨基酸掺入X - GPs就表明了这一点。再生神经中X - GPs的合成增加,这表明这些蛋白质可能在再生中起作用。对这些蛋白质的部分氨基酸测序表明,它们与先前鉴定为“室管膜蛋白”的蛋白质相同,这些蛋白质与神经元可塑性有关。一些个别斑点的氨基酸序列存在微小差异。